Data / Medical devices / United States / Chamberlain Technologies, LLC

Chamberlain Technologies, LLC: FDA-registered device maker in Deer Park, IL, United States, 4 510(k) clearances

Name: Chamberlain Technologies, LLC FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Chamberlain Technologies, LLC is registered with the FDA (registration 3015860534) in Deer Park, IL, United States. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 26, 2012. 1 recall event names it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3015860534
Address: 21805 W Field Parkway Suite 160, Deer Park, IL, United States, 60010
Owner or operator: Chamberlain Technologies, LLC (10061294)
Roles: Specification developer
First device listed: October 4, 2019
Registered through: 2026
Brand names listed: SurgiMesh WN, SurgiMesh XB, SurgiMesh XB Skirted, SurgiMesh XD

Devices it lists

Device	Product code	Class	Role	Source
Mesh, Surgical, Non-Absorbable, Large Abdominal Wall Defects	OXJ	2	Specification developer	accessdata.fda.gov
Mesh, Surgical, Polymeric	FTL	2	Specification developer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
June 26, 2012	K120025	SURGIMESH XB - SKIRTED	FTL	Substantially Equivalent	Aspide Medical	accessdata.fda.gov
June 25, 2010	K092233	SURGIMESH XD	FTL	Substantially Equivalent	Aspide Medical	accessdata.fda.gov
August 18, 2008	K072974	SURGIMESH XB	FTL	Substantially Equivalent	Aspide Medical	accessdata.fda.gov
February 1, 2007	K061445	SURGIMESH WN	FTL	Substantially Equivalent	Aspide Medical	accessdata.fda.gov

Recalls

Recall events where this establishment is the recalling firm, matched on its FEI.

Initiated	Event	Class	Status	Product	Reason	Source
August 12, 2022	96930	Class II	Completed	SURGIMESH WN, Polymeric Surgical Mesh, Large Flat Sheet, Model/Catalog Number: T3030	Potential presence of residual adhesive material on the mesh surface.	accessdata.fda.gov

Compare with other makers

Updated June 17, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.